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Tolstikov Genrikh A

Researcher at Russian Academy of Sciences

Publications -  1346
Citations -  5730

Tolstikov Genrikh A is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Catalysis & Ozonolysis. The author has an hindex of 27, co-authored 1346 publications receiving 5222 citations. Previous affiliations of Tolstikov Genrikh A include Bashkir State University.

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13C NMR spectra of biologically active compounds XI. Diastereomeric effects in C-glycosides

TL;DR: In this paper, the diastereomeric effects of the chemical shifts have been determined and assignments have been made to the 1α and 1β- stereochemical series on the basis of HH COSY and CH HET CORR two-dimensional NMR spectra.
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Alkaloids of Siberia and Altai flora: XVIII. Alkyl 2-acetylamino-5-[2-(pyridin-3-yl)vinyl]benzoates in the synthesis of indolizines containing an anthranilic acid ester moiety

TL;DR: In this article, 1,3-Dipolar cycloaddition of 1-(2-aryl-2-oxoethyl)-2-methyl-5-(4-acetylamino-3-methoxycarbonyl) pyridinium bromides with methyl propynoate was regioselective.
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Ozonolysis of (1R,cis)-4,7,7-Trimethyl-3-oxabicyclo[4.1.0]hept-4-en-2-one

TL;DR: The structure of peroxides forming in ozonolysis of enololactone and their further transformations are determined by the structure of the initial substrate and by effect of solvent used for ozonization as discussed by the authors.
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Synthesis of 2-amino-4-aryl-3-cyano-4H-pyrano and 2-amino-3-cyanothieno derivatives of cyclopentanonopimaric acid

TL;DR: Condensation of cyclopentanonopimaric acid with malononitrile in the presence of p-methoxybenzaldehyde or elemental sulfur gave the corresponding fused 2-amino-3-cyano-4-(4methoxyphenyl)-4H-pyrano derivatives.
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Transformations of Peroxide Products of Olefin Ozonolysis in Tetrahydrofuran in Reactions with Hydroxylamine and Semicarbazide Hydrochlorides

TL;DR: Treatment with hydroxylamine and semicarbazide hydrochlorides of peroxide products obtained by ozonolysis of olefins in tetrahydrofuran gives mainly carboxylic acids and their derivatives as mentioned in this paper.